TY  - GEN
AU  - Rittinger,Olaf
AU  - Krabichler,Birgit
AU  - Kronberger,Gabriela
AU  - Kotzot,Dieter
TI  - Clinical, cytogenetic, and molecular findings in a patient with a 46,XX,del(18)(q22)/46,XX,idic(18)(q22) karyotype
SN  - 1878-0849
PY  - 2016///0913
KW  - Chromosome Deletion
KW  - Chromosome Duplication
KW  - Chromosomes, Human, Pair 18
KW  - genetics
KW  - Cleft Palate
KW  - diagnosis
KW  - Craniofacial Abnormalities
KW  - Female
KW  - Heart Septal Defects, Ventricular
KW  - Humans
KW  - Infant
KW  - Karyotype
KW  - Mosaicism
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.ejmg.2015.09.011
ER  -